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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060608Generated: October 29, 2026

2-Methyl-2-butanol → HCID 44623807, compound

https://huagongshe.com/reaction/2060608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(6-Bromopyridin-2-yl)acetonitrileHCID 642864—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant5-Amino-2-[4-(1-hydroxy-1-methylethyl)phenyl]-1,3-thiazole-4-carboxamideHCID 58335264—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 44623807HCID 44623807—

Reaction Steps

The title compound was prepared as described in Example 1, Step 2 using 5-amino-2-[4-(1-hydroxy-1-methylethyl)phenyl]-1,3-thiazole-4-carboxamide (Example 5, Step 3) (150 mg, 0.54 mmol), (6-bromopyridin-2-yl)acetonitrile (107 mg, 0.54 mmol), Pd2(dba)3 (30 mg, 0.032 mmol), X-PHOS (77 mg, 0.16 mmol), potassium carbonate (82 mg, 0.60 mmol), and tert-amyl alcohol (1.2 ml) as starting materials. 1H NMR (600 MHz, d6-DMSO) δ 11.31 (s, 1H), 7.86 (d, 2H), 7.73 (m, 2H), 7.62 (s, 1H), 7.53 (d, 2H), 7.16 (d, 1H), 6.94 (d, 1H), 5.08 (s, 1H), 4.27 (s, 2H), 1.42 (s, 6H). LRMS (APCI) calc'd for C20H20N5O2S [M+H]+ 394.1, found 394.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278335B2
Source datasetuspto-grants-2012_10
ORD IDord-64931a4ef5f24874a288252ae29235ce
Source noteuspto-grants-2012_10